All of us with long Covid believe you!! Stay strong and find whatever will work for you. I pray that time will ease some of our symptoms. The people who love you will try and understand or at least do their own research on this subject for your sake 😊.
Thank you for another great video Naima. It is sad but so very true that long covid as well as all other invisible illnesses need to be recognized, validated, taken seriously and studied in depth! It truly is an epidemic that seems to be invisible to most. I live in Canada and now that the "pandemic " is no longer a problem, so they say, Long covid is still high risk...yet, since 2020 to now...the silence about long covid is astounding!! If I had not had access to UA-cam, I don't know where I would be right now!! That is a very sad reality for all of us, I think. Sending healing, positive energy your way. I hope that you are still doing better. Hugs ❤😊
Hi Kathy - you're completely right it's very sad for those of us going through it and it can feel like we live in a parallel world. Know that there are millions of us around the world who know exactly what this is like. Sending you healing and positivity too. Wish you all the best 💛🥰
Thanks Naima really thoughtful video. Much appreciated. I've lived most of my life with ME/CFS one of the biggest breakthroughs for me was accepting I had it and learning how to manage it. I've only just realised how much shame I feel at having devastating effects from Covid living now with Long Covid (added heart and dysautonomia symptoms,). I'm learning more now from the Long Covid community. Thanks again for all your hard work you make really good videos 😊
Sorry you've had to deal with ME/CFS and now long COVID as well - must be very difficult. I know the shame really crept up on me. It wasn't an emotion I was very familiar with, but it's definitely there a lot of the time. Hope you're having a good day 💛
Thank you both so much these replied are much appreciated. Although my nights feel very rough Im trying to make the most of the energies for the day. Yes Sibo is part of my journey too. Good luck with this. I found the food marble aire device very helpful identifying Sibo.
One of the problems with long COVID is that the government does not want to say that you can claim disability if you have long COVID...this is a key problem. I suffer from long COVID and it is disabling because I have to continue to work since I am self employed. I work in IT so I work from home but the problem is you need to be able to concentrate and this can be effected as the illness comes in waves, as you know. Recently went to hospital thinking I was having an heart attack but nothing showed up and all the tests were clear. I have shortness of breath and debilitating anxiety which is to do with high histamine buildup in the body. I was prescribed with famotidine which helped for around 2 weeks but then the side effect kicked in with this, which is rare but it happened to me ... Emptiness and depression. I stopped the famotidine and moved to quercetin (Solga) instead which helps but not as good as famotidine did...but it holds it at bay and makes things bearable. From the outside when people look at you they think your okay but inside your fighting a battle physically and mentally.
That sounds so difficult. I've heard in the US the people who have been ill for three years are only just getting their financial support. It sounds very difficult to navigate the bureaucracy too. I'm sorry famotidine didn't help me either. It made my fatigue so much worse. So much trial and error involved to find what works it can get exhausting. Exactly this is an invisible struggle and it makes it very hard for this illness to get the recognition it deserves given how many people are impacted.
Your channel was one of the first channels I ran across when I first suspected Long COVID in my own personal story - and I want to thank you for being a voice for LC. You inspired me to share my own story online, and here recently I’ve started to heal from Long COVID. I share this on my UA-cam and TikTok, and I wonder if the method of healing im doing could help you too. I wish you (and every long hauler) so much healing!
Thank you SO much for posting this! Turning the volume up for those around me who got the vaccine, a beyond selfish decision. Praying for their conviction and repentance. I will never stop warning people how dangerous this bio weapon is. We (husband and I) have both had long covid for about 2+ years now! Taking daily supplements of: Nattokinase, Serrapeptase, Lumbrokinase now for 5 about days.
Another great video, all very well said, you speak so well with authority and insight. I wish you, all of us, better health. Keep up, gently, kindly to yourself, the good work💜💜💜✌️✌️😊😊 The DWP, MPs, government don't seem to give a damn in the UK, they can be very cruel in fact, long Covid, (Acute Long Covid Syndrome) only interests them when they're using Long Covid as a nudging tactic or to cover up other "medical issues". In fact I'd argue that the DWP and it's - tail wagging the dog - subcontractors, are anti disability. The general public are too busy with bread and circuses and/or only see the disabled as those in Eg the Paralympics etc. A recent survey of the general public, of those surveyed, iirc, stated that 20% of the general public saw those who were sick and disabled as a burden to be gotten rid of! Hidden disabilities are subjected to a huge amount of prejudice💔💔 Before the plandemic health benefit fraud was about 0.05% (independently verified at 0.06%), yet when IDS rebranded various health benefits the cruelty factor went up several notches. So much so, that suicide rates went up too (see the hard to watch C4 Despatches programme) it got so bad that the UN were called in to investigate. Then came the bioweapon attack and everything was brushed under the carpet. Now, I'm not sure what health benefit fraud runs at, due in the main, to illegal immigration etc. But let's assume that such doesn't have an impact, there are a lot of sick people post the pandemic. I estimate that's there's at least 4 million of us in the UK, with a sliding scale of symptoms. Three years in and only now are some getting limited NHS help. The MSM, government et al are not interested, won't seek reparations from the CCP etc etc. There was little budget for M.E, FMS and MS research, slightly more for ALCS, but budgets for any of these are tiny in reality. Whilst ill most of us have had to fight every step of the way in a country that barely functions, okay we have some first world issues, but the treatment of those with ALCS is, at best, woefully and willfully inadequate 💔🤬💩💜☹️😥 Many of the sick are being gaslit or ghosted by their MPs too. A friend of mine states that one judges a country by its communication networks, Eg as Described by Adam Smith as including roads, and canals (back in the day) and how a country treats its most vulnerable, the sick, disabled and poor. Our roads are dire and the rest is worse off!💔😥☹️
I’m sorry. The uncertainty and length of time being unwell can be so scary. I’m three years in and have had lots of ups and downs. I hope things start to improve for you soon.
Nice seeing you again,I want to ask are you still on nattokinase,what was the effect and for how long did you use it .please I will love an update on this.Thanks
Hey no I stopped taking after about seven weeks. For me there were many ups and downs and the downs were very debilitating. Sadly it didn’t agree with me even though it’s helping so many people
Is anyone suffering from memory problems? My memory is so bad that I lose my chain of thoughts when I am speaking. I have a hard time focusing as well. Please let me know what supplements can help me?
Think of it as a hypersensitive nervous system and that's the reason your body didn't recover after a few weeks like it normally would Fix the nervous system and the body will heal naturally
@@naturespleasantries Type that into youtube or google and youll get some good answers. Me personally i changed my diet, used meditation, avoid stressful people etc
High doses of vitamin d3 I'm talking 50,000iu per day with 600mcg of k2, 600mg n-acetylcysteine 2x a day, bacopa, vinpocetine and melatonin at night will make anyone suffering from long covid (aka vaccine damage) feel a whole lot better real quick.
@@naimaella dang. I was considering taking it. Im a year and a half after covid. And i still have relapses in symptoms. For me the migraines are the worst part. Im 29, 185lbs, and bodybuild. But keep having to take numerous weeks off from the gym. Do you feel like LDN is helping you?
I am on both natto and ldn and both are helping me. Especially ldn it seems. Don't discount nattokinase - you may not have the effects Naima had... I don't...
Dame right. I’m long Covid and I felt I left behind on everything and no one believed me.
I’m sorry it’s very difficult. Sending you a virtual hug 🤗
All of us with long Covid believe you!! Stay strong and find whatever will work for you. I pray that time will ease some of our symptoms. The people who love you will try and understand or at least do their own research on this subject for your sake 😊.
Thank you for another great video Naima. It is sad but so very true that long covid as well as all other invisible illnesses need to be recognized, validated, taken seriously and studied in depth! It truly is an epidemic that seems to be invisible to most. I live in Canada and now that the "pandemic " is no longer a problem, so they say, Long covid is still high risk...yet, since 2020 to now...the silence about long covid is astounding!! If I had not had access to UA-cam, I don't know where I would be right now!! That is a very sad reality for all of us, I think. Sending healing, positive energy your way. I hope that you are still doing better. Hugs ❤😊
Hi Kathy - you're completely right it's very sad for those of us going through it and it can feel like we live in a parallel world. Know that there are millions of us around the world who know exactly what this is like.
Sending you healing and positivity too. Wish you all the best 💛🥰
Thanks Naima really thoughtful video. Much appreciated. I've lived most of my life with ME/CFS one of the biggest breakthroughs for me was accepting I had it and learning how to manage it. I've only just realised how much shame I feel at having devastating effects from Covid living now with Long Covid (added heart and dysautonomia symptoms,). I'm learning more now from the Long Covid community. Thanks again for all your hard work you make really good videos 😊
Sorry you've had to deal with ME/CFS and now long COVID as well - must be very difficult.
I know the shame really crept up on me. It wasn't an emotion I was very familiar with, but it's definitely there a lot of the time.
Hope you're having a good day 💛
Bless you. Ditto here too. SIBO testing is next on the very long list. I wish you a speedy recovery 💜💜✌️✌️😊😊
Thank you both so much these replied are much appreciated. Although my nights feel very rough Im trying to make the most of the energies for the day. Yes Sibo is part of my journey too. Good luck with this. I found the food marble aire device very helpful identifying Sibo.
One of the problems with long COVID is that the government does not want to say that you can claim disability if you have long COVID...this is a key problem. I suffer from long COVID and it is disabling because I have to continue to work since I am self employed. I work in IT so I work from home but the problem is you need to be able to concentrate and this can be effected as the illness comes in waves, as you know.
Recently went to hospital thinking I was having an heart attack but nothing showed up and all the tests were clear. I have shortness of breath and debilitating anxiety which is to do with high histamine buildup in the body. I was prescribed with famotidine which helped for around 2 weeks but then the side effect kicked in with this, which is rare but it happened to me ... Emptiness and depression. I stopped the famotidine and moved to quercetin (Solga) instead which helps but not as good as famotidine did...but it holds it at bay and makes things bearable.
From the outside when people look at you they think your okay but inside your fighting a battle physically and mentally.
That sounds so difficult. I've heard in the US the people who have been ill for three years are only just getting their financial support. It sounds very difficult to navigate the bureaucracy too.
I'm sorry famotidine didn't help me either. It made my fatigue so much worse. So much trial and error involved to find what works it can get exhausting.
Exactly this is an invisible struggle and it makes it very hard for this illness to get the recognition it deserves given how many people are impacted.
Your channel was one of the first channels I ran across when I first suspected Long COVID in my own personal story - and I want to thank you for being a voice for LC.
You inspired me to share my own story online, and here recently I’ve started to heal from Long COVID. I share this on my UA-cam and TikTok, and I wonder if the method of healing im doing could help you too.
I wish you (and every long hauler) so much healing!
I have long COVID as well. I like seeing your new videos as it gives me another opinion.
And this video rang so true.
Thanks Cynthia. Hope your recovery is going ok! 💛
Thank you SO much for posting this! Turning the volume up for those around me who got the vaccine, a beyond selfish decision. Praying for their conviction and repentance. I will never stop warning people how dangerous this bio weapon is. We (husband and I) have both had long covid for about 2+ years now! Taking daily supplements of: Nattokinase, Serrapeptase, Lumbrokinase now for 5 about days.
Another great video, all very well said, you speak so well with authority and insight. I wish you, all of us, better health. Keep up, gently, kindly to yourself, the good work💜💜💜✌️✌️😊😊
The DWP, MPs, government don't seem to give a damn in the UK, they can be very cruel in fact, long Covid, (Acute Long Covid Syndrome) only interests them when they're using Long Covid as a nudging tactic or to cover up other "medical issues". In fact I'd argue that the DWP and it's - tail wagging the dog - subcontractors, are anti disability.
The general public are too busy with bread and circuses and/or only see the disabled as those in Eg the Paralympics etc. A recent survey of the general public, of those surveyed, iirc, stated that 20% of the general public saw those who were sick and disabled as a burden to be gotten rid of! Hidden disabilities are subjected to a huge amount of prejudice💔💔
Before the plandemic health benefit fraud was about 0.05% (independently verified at 0.06%), yet when IDS rebranded various health benefits the cruelty factor went up several notches. So much so, that suicide rates went up too (see the hard to watch C4 Despatches programme) it got so bad that the UN were called in to investigate. Then came the bioweapon attack and everything was brushed under the carpet. Now, I'm not sure what health benefit fraud runs at, due in the main, to illegal immigration etc. But let's assume that such doesn't have an impact, there are a lot of sick people post the pandemic. I estimate that's there's at least 4 million of us in the UK, with a sliding scale of symptoms. Three years in and only now are some getting limited NHS help. The MSM, government et al are not interested, won't seek reparations from the CCP etc etc. There was little budget for M.E, FMS and MS research, slightly more for ALCS, but budgets for any of these are tiny in reality.
Whilst ill most of us have had to fight every step of the way in a country that barely functions, okay we have some first world issues, but the treatment of those with ALCS is, at best, woefully and willfully inadequate 💔🤬💩💜☹️😥
Many of the sick are being gaslit or ghosted by their MPs too. A friend of mine states that one judges a country by its communication networks, Eg as Described by Adam Smith as including roads, and canals (back in the day) and how a country treats its most vulnerable, the sick, disabled and poor. Our roads are dire and the rest is worse off!💔😥☹️
Thanks I wish you better health too. Sending you a virtual hug and be kind to yourself as well 💛😊
@@naimaella Ahh bless you, thank you💜💜 back at you too💜💜💜✌️✌️👍😊😊
22 months post covid and if anything I’m getting worse, simply down to disbelief
I’m sorry. The uncertainty and length of time being unwell can be so scary. I’m three years in and have had lots of ups and downs. I hope things start to improve for you soon.
@@naimaella Thanks, So do I, I've not been able to work since taking I'll. It's certainly been a life changer
Nice seeing you again,I want to ask are you still on nattokinase,what was the effect and for how long did you use it .please I will love an update on this.Thanks
Hey no I stopped taking after about seven weeks. For me there were many ups and downs and the downs were very debilitating. Sadly it didn’t agree with me even though it’s helping so many people
Is anyone suffering from memory problems? My memory is so bad that I lose my chain of thoughts when I am speaking. I have a hard time focusing as well. Please let me know what supplements can help me?
I got relief from doing 14/8 intermittent fasting and cutting down on sugar. Magnesium Threonate I found good for my brain.
Think of it as a hypersensitive nervous system and that's the reason your body didn't recover after a few weeks like it normally would
Fix the nervous system and the body will heal naturally
How do you heal the nervous system
@@naturespleasantries Type that into youtube or google and youll get some good answers.
Me personally i changed my diet, used meditation, avoid stressful people etc
High doses of vitamin d3 I'm talking 50,000iu per day with 600mcg of k2, 600mg n-acetylcysteine 2x a day, bacopa, vinpocetine and melatonin at night will make anyone suffering from long covid (aka vaccine damage) feel a whole lot better real quick.
These people are victims they refuse to believe it’s their own way to healing. Lol
Are you still on nattokinase?
No I stopped after 7/8 weeks. It caused me to have intense highs and lows and the lows were way too debilitating.
@@naimaella dang. I was considering taking it. Im a year and a half after covid. And i still have relapses in symptoms. For me the migraines are the worst part. Im 29, 185lbs, and bodybuild. But keep having to take numerous weeks off from the gym. Do you feel like LDN is helping you?
@@AngelofD69 it's different for everyone and does seem to really help some people. LDN is really helping me so far - especially with PEM and fatigue.
I am on both natto and ldn and both are helping me. Especially ldn it seems. Don't discount nattokinase - you may not have the effects Naima had... I don't...